HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400189Generated: November 3, 2026
Dicyclohexylcarbodiimide → Methyl 4-(Acetylamino)-3-[(Acetoxyacetyl)Amino]Benzoate
https://huagongshe.com/reaction/2400189
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Acetoxyacetic acid | HCID 83766 | — |
| Reactant | Methyl 4-(Acetylamino)-3-Aminobenzoate, Hydrochloride | HCID 131719127 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 4-(Acetylamino)-3-[(Acetoxyacetyl)Amino]Benzoate | HCID 10447968 | 678.9% |
Reaction Steps
Compound 16 (0.20 g, 0.96 mmol) was dissolved in a mixture of anhydrous DMF (2 mL) and anhydrous dioxane (5 mL), and the solution was cooled to 0°-5° C. in an ice bath. To this were added acetoxy acetic acid (0.124 g, 0.129 mmol) and DCC (0.198 g, 0.210 mL, 0.960 mmol). The reaction mixture was stirred for a few minutes at 0° C., the ice bath was removed, and the mixture was stirred at room temperature for 4 hours. The solid which separated was filtered and the filtrate was concentrated to dryness on a rotary evaporator. The solid residue was triturated with 5% HCl, filtered, and washed on the filter with water. The collected solid was then triturated with 5% NaHCO3, filtered, washed with water, and dried under vacuum to give 17 (270 mg, 70.9% yield) as a white solid: mp 182°-186° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05453533 |
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| Source dataset | uspto-grants-1995_09 |
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| ORD ID | ord-b32e9ee7d80643fea964f7859731fe54 |
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| Source note | uspto-grants-1995_09 |
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